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FDA 510(k)

M-FLEX 5000 C3PMD

K-Number: K931736 · 1994-01-27

ApplicantMedical Systems Corp.
Decision Date1994-01-27
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

M-FLEX 5000 C3PMD is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Corp.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K931736. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M-FLEX 5000 C3PMD?

M-FLEX 5000 C3PMD is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Medical Systems Corp.. The 510(k) number is K931736.

When did M-FLEX 5000 C3PMD receive FDA 510(k) clearance?

M-FLEX 5000 C3PMD received FDA 510(k) clearance on 1994-01-27, under 510(k) number K931736.

Who is the listed applicant for M-FLEX 5000 C3PMD?

The FDA 510(k) record lists Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M-FLEX 5000 C3PMD?

The FDA product code for M-FLEX 5000 C3PMD is BXB.

Other records listing Medical Systems Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K921513SPIROLITE MODEL MSC-201 SPIROMETERK921485LA MONT VIDEO PATIENT MONITORING SYSTEMK904353CARDIOMATIC MODEL MSC-2001K903501RADIANT TEMPERATUR INDICATOR MODEL 25EK902192MODEL MSC SA02-5000 PULSE OXIMETERK902608CARDIOMATIC MODEL MSC-1001

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Related Devices (Code: BXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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